Variant #0000357060 (NC_000002.11:g.48023128A>G, NM_000179.2:c.553A>G (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48023128A>G
DNA change (hg38) g.47795989A>G
Published as -
ISCN -
DB-ID MSH6_000631 See all 2 reported entries
Variant remarks Insight class: 3
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2018-03-08 19:39:55 +01:00 (CET)
Date last edited 2018-11-09 16:06:39 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 ?/? 3 c.553A>G r.(?) p.(Lys185Glu)


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